A method of doping with yttrium to induce crystal transformation of bismuth oxide to improve its photocatalytic effect
A technology of crystal transformation and bismuth oxide, applied in the direction of metal/metal oxide/metal hydroxide catalysts, chemical instruments and methods, physical/chemical process catalysts, etc., can solve the problem of low migration efficiency and easy recombination of photogenerated carriers , Utilization rate is not high, to overcome the effects of easy compounding, high light energy utilization efficiency, and low cost
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Embodiment 1
[0023] Dissolve 66 grams of bismuth nitrate in 500 grams of absolute ethanol, adjust the acidity to pH 1-2 with commercially available 38% concentrated nitric acid, and add 8.5 grams of cetyltrimethylammonium bromide as a dispersant. Stir slowly until complete dissolution and store at room temperature for 24 hours to achieve seed induction. Add 7 grams of yttrium nitrate into 10 ml of nitric acid aqueous solution with a mass concentration of 10%, slowly heat until completely dissolved, slowly add this solution into the aforementioned bismuth nitrate solution, keep stirring, and control the stirring speed at 200 rpm until completely dispersed , a pale orange-yellow suspension was formed, and stirring was continued at room temperature for 3 hours. The obtained solution was transferred to a high-temperature crystallization kettle with a polytetrafluoroethylene liner, sealed and stored in an oven, and the temperature of the oven was set at 150°C. After 24 hours, the obtained preci...
Embodiment 2
[0027] Dissolve 73 grams of bismuth nitrate in 500 grams of absolute ethanol, adjust the acidity to pH 1-2 with commercially available 38% concentrated nitric acid, add 10.2 grams of cetyltrimethylammonium bromide, and stir slowly until completely dissolved , preserved for 24 hours; 5 grams of yttrium nitrate was added in 10 milliliters of 10% nitric acid aqueous solution, heated to dissolve, slowly added to the aforementioned bismuth nitrate solution, stirred and dispersed to form a light orange-yellow suspension, and after continuous stirring for 3 hours, Transfer to a crystallization kettle, crystallize at 150°C for 24 hours, and the obtained precipitate is filtered, washed, dried, and calcined at 500°C for 3 hours to obtain a bismuth oxide photocatalyst induced by yttrium doping to achieve crystal transformation. Details of the remaining synthesis steps and activity evaluation steps are the same as in Example 1.
[0028] The photocatalyst identified by X-ray diffraction is...
Embodiment 3
[0030] Dissolve 106 grams of bismuth nitrate in 500 grams of absolute ethanol, adjust the acidity to pH 1-2 with commercially available 38% concentrated nitric acid, add 11.7 grams of cetyltrimethylammonium bromide, and stir slowly until completely dissolved , stored for 24 hours; 10 grams of yttrium nitrate was added in 10 milliliters of 10% nitric acid aqueous solution, heated to dissolve, slowly added to the aforementioned bismuth nitrate solution, stirred and dispersed to form a light orange-yellow suspension, and after continuous stirring for 3 hours, Transfer to a crystallization kettle, crystallize at 150°C for 24 hours, and the obtained precipitate is filtered, washed, dried, and calcined at 575°C for 3 hours to obtain a bismuth oxide photocatalyst induced by yttrium doping to achieve crystal transformation. Details of the remaining synthesis steps and activity evaluation steps are the same as in Example 1.
[0031] The obtained photocatalyst was identified by X-ray di...
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